肝再生
再生(生物学)
祖细胞
刺猬
生物
细胞生物学
刺猬信号通路
器官发生
肝切除术
肝损伤
祖细胞
干细胞
内分泌学
内科学
信号转导
医学
生物化学
外科
切除术
基因
作者
Begoña Ochoa,Wing‐Kin Syn,Igotz Delgado,Gamze Karaca,Youngmi Jung,Jiangbo Wang,Ana M. Zubiaga,Olatz Fresnedo,Alessia Omenetti,Marzena Zdanowicz,Steve S. Choi,Anna Mae Diehl
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2010-01-15
卷期号:51 (5): 1712-1723
被引量:181
摘要
Distinct mechanisms are believed to regulate growth of the liver during fetal development and after injury in adults, because the former relies on progenitors and the latter generally involves replication of mature hepatocytes. However, chronic liver injury in adults increases production of Hedgehog (Hh) ligands, developmental morphogens that control progenitor cell fate and orchestrate various aspects of tissue construction during embryogenesis. This raises the possibility that similar Hh-dependent mechanisms also might regulate adult liver regeneration. The current analysis of murine liver regeneration after 70% partial hepatectomy (PH), an established model of adult liver regeneration, demonstrated that PH induced production of Hh ligands and activated Hh signaling in liver cells. Treatment with a specific Hh signaling inhibitor interfered with several key components of normal liver regeneration, significantly inhibiting progenitor responses, matrix remodeling, proliferation of hepatocytes and ductular cells, and restoration of liver mass. These global inhibitory effects on liver regeneration dramatically reduced survival after PH. Conclusion: Mechanisms that mediate liver organogenesis, such as Hh pathway activation, are retained and promote reconstruction of adult livers after injury. Hepatology 2010
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